{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["24(10)"],"submitter":["Marconi GD"],"pubmed_abstract":["Gliomas are malignant brain tumors characterized by rapid spread and growth into neighboring tissues and graded I-IV by the World Health Organization. Glioblastoma is the fastest growing and most devastating IV glioma. The aim of this paper is to evaluate the biological effects of two potent and selective Monoamine Oxidase B (MAO-B) inhibitors, Cmp3 and Cmp5, in C6 glioma cells and in CTX/TNA2 astrocytes in terms of cell proliferation, apoptosis occurrence, inflammatory events and cell migration. These compounds decrease C6 glioma cells viability sparing normal astrocytes. Cell cycle analysis, the Mitochondrial Membrane Potential (MMP) and Reactive Oxygen Species (ROS) production were detected, revealing that Cmp3 and Cmp5 induce a G1 or G2/M cell cycle arrest, as well as a MMP depolarizat"],"journal":["Molecules (Basel, Switzerland)"],"pagination":["E2005"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC6572653"],"repository":["biostudies-literature"],"pubmed_title":["The Up-Regulation of Oxidative Stress as a Potential Mechanism of Novel MAO-B Inhibitors for Glioblastoma Treatment."],"pmcid":["PMC6572653"],"pubmed_authors":["Gallorini M","Cataldi A","Marconi GD","Carradori S","Zara S","Guglielmi P"],"additional_accession":[]},"is_claimable":false,"name":"The Up-Regulation of Oxidative Stress as a Potential Mechanism of Novel MAO-B Inhibitors for Glioblastoma Treatment.","description":"Gliomas are malignant brain tumors characterized by rapid spread and growth into neighboring tissues and graded I-IV by the World Health Organization. Glioblastoma is the fastest growing and most devastating IV glioma. The aim of this paper is to evaluate the biological effects of two potent and selective Monoamine Oxidase B (MAO-B) inhibitors, Cmp3 and Cmp5, in C6 glioma cells and in CTX/TNA2 astrocytes in terms of cell proliferation, apoptosis occurrence, inflammatory events and cell migration. These compounds decrease C6 glioma cells viability sparing normal astrocytes. Cell cycle analysis, the Mitochondrial Membrane Potential (MMP) and Reactive Oxygen Species (ROS) production were detected, revealing that Cmp3 and Cmp5 induce a G1 or G2/M cell cycle arrest, as well as a MMP depolarizat","dates":{"release":"2019-01-01T00:00:00Z","publication":"2019 May","modification":"2025-04-26T06:30:35.565Z","creation":"2019-07-24T07:19:40Z"},"accession":"S-EPMC6572653","cross_references":{"pubmed":["31130597"],"doi":["10.3390/molecules24102005"]}}